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Deprotection, Tethering, and Activation of a Catalytically Active Metalloporphyrin to a Chemically Active Metal Surface: [SAc]4P−Mn(III)Cl on Ag(100)
Author(s) -
Mark Turner,
Owain Vaughan,
Georgios Kyriakou,
David J. Watson,
Lukas J. Scherer,
G.J.E. Davidson,
Jeremy K. M. Sanders,
Richard M. Lambert
Publication year - 2009
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja8076389
Subject(s) - chemistry , porphyrin , desorption , catalysis , chlorine , manganese , adsorption , covalent bond , ligand (biochemistry) , thermal desorption , metal , x ray photoelectron spectroscopy , photochemistry , thermal desorption spectroscopy , inorganic chemistry , polymer chemistry , organic chemistry , chemical engineering , receptor , biochemistry , engineering
The adsorption and subsequent thermal chemistry of the acetyl-protected manganese porphyrin, [SAc](4)P-Mn(III)Cl on Ag(100) have been studied by high resolution XPS and temperature-programmed desorption. The deprotection event, leading to formation of the covalently bound thioporphyrin, has been characterized and the conditions necessary for removal of the axial chlorine ligand have been determined, thus establishing a methodology for creating tethered activated species that could serve as catalytic sites for delicate oxidation reactions. Surface-mediated acetyl deprotection occurs at 298 K, at which temperature porphyrin diffusion is limited. At temperatures above approximately 425 K porphyrin desorption, diffusion and deprotection occur and at >470 K the axial chlorine is removed.

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